美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
57664-508-13	57664-508	HUMAN PRESCRIPTION DRUG	citalopram hydrobromide	citalopram hydrobromide	TABLET	ORAL	20150529	N/A	ANDA	ANDA077032	Sun Pharmaceutical Industries, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	500 TABLET in 1 BOTTLE (57664-508-13)
57664-508-18	57664-508	HUMAN PRESCRIPTION DRUG	citalopram hydrobromide	citalopram hydrobromide	TABLET	ORAL	20150529	N/A	ANDA	ANDA077032	Sun Pharmaceutical Industries, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	1000 TABLET in 1 BOTTLE (57664-508-18)
57664-508-88	57664-508	HUMAN PRESCRIPTION DRUG	citalopram hydrobromide	citalopram hydrobromide	TABLET	ORAL	20150529	N/A	ANDA	ANDA077032	Sun Pharmaceutical Industries, Inc.	CITALOPRAM HYDROBROMIDE	20 mg/1	100 TABLET in 1 BOTTLE (57664-508-88)
57664-507-13	57664-507	HUMAN PRESCRIPTION DRUG	citalopram hydrobromide	citalopram hydrobromide	TABLET	ORAL	20150529	N/A	ANDA	ANDA077032	Sun Pharmaceutical Industries, Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	500 TABLET in 1 BOTTLE (57664-507-13)
57664-507-88	57664-507	HUMAN PRESCRIPTION DRUG	citalopram hydrobromide	citalopram hydrobromide	TABLET	ORAL	20150529	N/A	ANDA	ANDA077032	Sun Pharmaceutical Industries, Inc.	CITALOPRAM HYDROBROMIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-507-88)